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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126470copy number variation1nstd186human GRCh37 chr18: 8,634,165-8,634,279 , GRCh38.p12 chr18: 8,634,167-8,634,281 RAB12
    nsv5931430copy number variation1nstd209human GRCh38 chr18: 8,634,166-8,634,280 , GRCh37.p13 chr18: 8,634,164-8,634,278 RAB12
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5588276copy number variation1nstd207human GRCh38 chr18: 8,634,166-8,634,280 , GRCh37.p13 chr18: 8,634,164-8,634,278 RAB12
    nsv5531417copy number variation1nstd206human GRCh38 chr18: 8,634,167-8,634,281 , GRCh37.p13 chr18: 8,634,165-8,634,279 RAB12
    nsv5382684mobile element deletion2nstd186human GRCh37 chr18: 8,634,165-8,634,279 , GRCh38.p12 chr18: 8,634,167-8,634,281 RAB12
    nsv5211846mobile element deletion1nstd204human GRCh38.p13 chr18: 8,634,167-8,634,281 , GRCh37.p13 chr18: 8,634,165-8,634,279 RAB12
    nsv5148466mobile element insertion1nstd203human GRCh38 chr18: 8,639,147-8,639,192 , GRCh37.p13 chr18: 8,639,145-8,639,190 RAB12
    nsv5014259copy number variation1nstd200human GRCh38 chr18: 8,325,854-8,971,614 , GRCh37.p13 chr18: 8,325,852-8,971,612 THEMIS3P, TOMM20P3, 8 more genes
    nsv5014258copy number variation1nstd200human GRCh38 chr18: 8,208,242-8,865,416 , GRCh37.p13 chr18: 8,208,240-8,865,414 PTPRM, COP1P1, 8 more genes
    nsv4907399mobile element deletion1nstd200human GRCh38 chr18: 8,634,167-8,634,281 , GRCh37.p13 chr18: 8,634,165-8,634,279 RAB12
    nsv4854524copy number variation1nstd200human GRCh37 chr18: 8,208,240-8,865,414 , GRCh38.p12 chr18: 8,208,242-8,865,416 RN7SL50P, GACAT2, 8 more genes
    nsv4769599mobile element deletion1nstd200human GRCh37 chr18: 8,634,165-8,634,279 , GRCh38.p12 chr18: 8,634,167-8,634,281 RAB12
    nsv4744384copy number variation1nstd199human GRCh37 chr18: 8,634,159-8,634,278 , GRCh38.p12 chr18: 8,634,161-8,634,280 RAB12
    nsv4729915copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,598,173-15,422,644 , GRCh38.p12 chr18: 7,598,175-15,410,899 CEP192, RNU2-27P, 155 more genes
    nsv4729833copy number variation1nstd102humanUncertain significance GRCh37 chr18: 7,180,048-8,727,482 , GRCh38.p12 chr18: 7,180,050-8,727,484 AKR1B1P6, LOC112577592, 15 more genes
    nsv4676396copy number variation1nstd102humanPathogenic GRCh37 chr18: 971,295-11,250,447 , GRCh38.p12 chr18: 971,294-11,250,448 LOC100129774, LOC100419892, 146 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PRELID3A, ANKRD30B, 275 more genes
    nsv4676314copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715 EIF4A2P1, PMM2P2, 263 more genes
    nsv4676159copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-13,894,429 , GRCh38.p12 chr18: 136,226-13,894,430 SLC25A51P2, BOLA2P1, 221 more genes
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